Imaging Ion Channel Dynamics in Living Neurons by Fluorescence Microscopy

Author(s):  
Barry W. Hicks ◽  
Kimon J. Angelides
2010 ◽  
Vol 1 (1) ◽  
pp. 1587-1596 ◽  
Author(s):  
C.E. Dangerfield ◽  
D. Kay ◽  
K. Burrage

Author(s):  
Ziqi Pi ◽  
Giovanni Zocchi

Abstract The Artificial Axon is a unique synthetic system, based on biomolecular components, which supports action potentials. Here we examine, experimentally and theoretically, the properties of the threshold for firing in this system. As in real neurons, this threshold corresponds to the critical point of a saddle-node bifurcation. We measure the delay time for firing as a function of the distance to threshold, recovering the expected scaling exponent of −1/2. We introduce a minimal model of the Morris-Lecar type, validate it on the experiments, and use it to extend analytical results obtained in the limit of ”fast” ion channel dynamics. In particular, we discuss the dependence of the firing threshold on the number of channels. The Artificial Axon is a simplified system, an Ur-neuron, relying on only one ion channel species for functioning. Nonetheless, universal properties such as the action potential behavior near threshold are the same as in real neurons. Thus we may think of the Artificial Axon as a cell-free breadboard for electrophysiology research.


2011 ◽  
Vol 694 ◽  
pp. 54-58
Author(s):  
Xin Liang Zhao ◽  
Xiao Liu ◽  
Hu Jie Lu ◽  
Li Ying Ma ◽  
Rui Ling Gao ◽  
...  

Continuous high-resolution observations of cell membrane would greatly aid the elucidation of the relationship between structure and function and facilitate the study of physiological processing in cell biology. However, high-resolution studying living neuron membrane structures and its functions is still a challenge in current nanobiology. The new developed Hoping Probe Ion Conductance Microscopy (HPICM) is designed for non-contact continuous high-resolution topographic imaging of living cells under physiological conditions. In this review, we concisely introduced the basic operation principle of HPICM and its applications in high spatial resolution imaging of two living neuron cell models, N-type SK-N-SH cells and NGF-differentiated sympathetic neuron-like PC12 cells. Combining HPICM with patch-clamp technique, we further investigated the functional ion-channel of under-differentiated neuron-like PC12 cells and demonstrated that NGF treatment promoted the outgrowth of neurites and increased the activity of TTX-sensitive sodium channel. All these results demonstrate that HPICM combined with patch-clamp technique offers high-resolution topographic imaging of living neurons with non-contact — making HPICM an ideal high-resolution imaging technique not to interact/interfere with living neurons during image acquisition, and provides detailed information about the relationship between membrane structures and ion-channel functions of living neurons at the same time, which has the potential to become a powerful microscopy for in-depth researching in neural nanobiology.


2015 ◽  
Vol 599 ◽  
pp. 34-46 ◽  
Author(s):  
Md. Ariful Islam ◽  
Abhishek Murthy ◽  
Ezio Bartocci ◽  
Elizabeth M. Cherry ◽  
Flavio H. Fenton ◽  
...  

2020 ◽  
Author(s):  
Erhui Wang ◽  
Liancun Zheng ◽  
Xuelan Zhang ◽  
Kheder Suleiman ◽  
Chang Shu

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